Global Alliance for Genomics and Health

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The Global Alliance for Genomics and Health (GA4GH) is an international consortium that is developing standards for responsibly collecting, storing, analyzing, and sharing genomic data in order to enable an "internet of genomics". [1] [2] GA4GH was founded in 2013. [3]

Contents

GA4GH is founded on the Framework for the Responsible Sharing of Genomic and Health-related Data, [4] which is based on the human right to benefit from scientific advances. [5]

Organization

GA4GH maintained by four Host Institutions (Wellcome Sanger Institute, Broad Institute, Ontario Institute for Cancer Research and the European Bioinformatics Institute). [6] Heidi Rehm is the current GA4GH chair [7] and Peter Goodhand is the Chief Executive Officer. [8] Kathryn North is the current Vice Chair and Ewan Birney is the past chair. [9]

Organizational members of the alliance include: [6]

Funding

GA4GH is supported by a "Funder's Forum" composed of organizations whose funding commitments exceed USD $200,000 annually, for at least three years. Forum members include: [6]

Activities

All GA4GH standards are developed by six technical and two foundational "Work Streams" in collaboration with real-world genomic data initiatives called "Driver Projects." [8]

GA4GH Work Streams

  1. Regulatory and Ethics (foundational) [7]  
  2. Data Security (foundational) [7]  
  3. Cloud Archived 2020-10-04 at the Wayback Machine [7]  
  4. Clinical & Phenotypic Data Capture [7]  
  5. Data Use and Researcher Identities [7]  
  6. Discovery Archived 2018-10-26 at the Wayback Machine [7]  
  7. Genomic Knowledge Standards [7]  
  8. Large Scale Genomics Archived 2020-09-21 at the Wayback Machine [7]  

GA4GH Driver Projects

  1. All of US Research Program [3]
  2. Australian Genomics [3]
  3. BRCA Challenge [3]
  4. Canadian Distributed Infrastructure for Genomics (CanDig) [3]
  5. Clinical Genome Resource (ClinGen) [3]
  6. ELIXIR Beacon [3]
  7. The European Nucleotide Archive, European Variation Archive, and European Genome-phenome Archive at EMBL-EBI [3]
  8. EUCANCan [10]
  9. European Joint Programme on Rare Diseases [11]
  10. Genomics England [12]
  11. Human Cell Atlas [12]
  12. Human Heredity and Health in Africa (H3Africa) [13]
  13. International Cancer Genome Consortium - ARGO [12]
  14. Matchmaker Exchange [12]
  15. The Monarch Initiative [12]
  16. National Cancer Institute Data Commons Framework (NCI DCF) and Genomic Data Commons (NCI GDC) [12]
  17. Trans-Omics for Precision Medicine (TOPMed) [12]
  18. Variant Interpretation for Cancer Consortium (VICC) Archived 2021-11-19 at the Wayback Machine [12]

Genomic Beacon API

The Genomic Beacon API is a standard of GA4GH. [14] The "Beacon" protocol was originally proposed as a simple standard for the discovery of genomic sequence variants using federated queries against a potentially large number of genomic databases with implicit security provided through the use of limited query parameters and restriction to Boolean responses. In the version 2 of the protocol the API supports "phenoclinical" queries (e.g. combining parameters for genomic variant discovery with diagnostic or technical parameters) as well as responses containing versions of the matched records.

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Knome, Inc. was a human genome interpretation company based in Cambridge, Massachusetts. Launched in 2007, Knome focused on improving quality of life by applying insights gained from the interpretation of human genomes. They helped identify and classify the variants, genes, and gene sets that are likely to govern or underlie a specific disease, tumor, or drug response. Their clients included academic, pharmaceutical and medical researchers. In 2015, it was acquired by Tute Genomics.

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Philip Awadalla is a professor of medical and population genetics at the Ontario Institute for Cancer Research, and the Department of Molecular Genetics, Faculty of Medicine, University of Toronto. He is the National Scientific Director of the Canadian Partnership for Tomorrow's Health (CanPath), formerly the Canadian Partnership for Tomorrow Project (CPTP), and executive director of the Ontario Health Study. He is also the Executive Scientific Director of the Genome Canada Genome Technology Platform, the Canadian Data Integration Centre. Professor Awadalla was the Executive Scientific Director of the CARTaGENE biobank, a regional cohort member of the CPTP, from 2009 to 2015, and is currently a scientific advisor for this and other scientific and industry platforms. At the OICR, he is Director of Computational Biology.

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Charmaine DM Royal is an American geneticist and Associate Professor at the Institute for Genome Sciences & Policy and the Department of African and African American Studies at Duke University. She studies the intersections of race, ethnicity, ancestry genetics, and health, especially as they pertain to historically marginalized and underrepresented groups in genetic and genomic research; and genomics and global health. Her major interest is in addressing root causes and implementing sustainable solutions regarding problems of race and racism in research, healthcare, and society. Royal is a Human Heredity and Health in Africa (H3Africa) Independent Expert Committee (IEC) member appointed by the National Institutes of Health (NIH) and is a 2020 Ida Cordelia Beam Distinguished Visiting Professor at the University of Iowa.

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References

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